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重症肌无力患者中的 CD4 FoxP3 T 调节性细胞亚群。

CD4 FoxP3 T regulatory cell subsets in myasthenia gravis patients.

机构信息

Department of Experimental Neurology, Charité, Campus Mitte, Charitéplatz 1, 10117 Berlin, Germany; Department of Neurology, Charité, Campus Mitte, Charitéplatz 1, 10117 Berlin, Germany; NeuroCure Clinical Research Center, Charité, Campus Mitte, Charitéplatz 1, 10117 Berlin, Germany.

Department of Experimental Neurology, Charité, Campus Mitte, Charitéplatz 1, 10117 Berlin, Germany; NeuroCure Clinical Research Center, Charité, Campus Mitte, Charitéplatz 1, 10117 Berlin, Germany.

出版信息

Clin Immunol. 2017 Jun;179:40-46. doi: 10.1016/j.clim.2017.03.003. Epub 2017 Mar 9.

Abstract

Although myasthenia gravis (MG) is a classic autoantibody-mediated disease, T cells are centrally involved in its pathogenesis. In recent years a number of studies have analyzed the role of CD4 FoxP3 regulatory T cells (T) in the disease with contradictory results. Here, the generation of T was significantly reduced in thymoma as compared to thymic hyperplasia and normal thymus tissue (p=0.0002). In the peripheral blood, T subsets classified according to CD49d, HELIOS and CD45RA expression changed after thymectomy and in the long-term course of immunosuppression. Compared to healthy volunteers the frequency of CD45RAFoxP3 T was reduced in MG patients in general (p=0.037) and in particular in patients without immunosuppression (p=0.036). In our study, thymectomy and immunosuppressive treatment were associated with changes in T subpopulations. The reduced frequency of CD45RAFoxP3 T we observed in MG patients might play a role in MG pathogenesis.

摘要

尽管重症肌无力 (MG) 是一种经典的自身抗体介导的疾病,但 T 细胞在其发病机制中起着核心作用。近年来,许多研究分析了 CD4 FoxP3 调节性 T 细胞 (T) 在疾病中的作用,但结果存在矛盾。在这里,与胸腺增生和正常胸腺组织相比,胸腺瘤中的 T 生成明显减少 (p=0.0002)。在外周血中,根据 CD49d、HELIOS 和 CD45RA 表达分类的 T 亚群在胸腺切除术后和长期免疫抑制过程中发生变化。与健康志愿者相比,MG 患者的 CD45RAFoxP3 T 频率普遍降低 (p=0.037),尤其是在未接受免疫抑制治疗的患者中 (p=0.036)。在我们的研究中,胸腺切除术和免疫抑制治疗与 T 亚群的变化相关。我们在 MG 患者中观察到的 CD45RAFoxP3 T 频率降低可能在 MG 的发病机制中起作用。

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